Reply: A homozygous GDAP2 loss-of-function variant in a patient with adult-onset cerebellar ataxia; and Novel GDAP2 pathogenic variants cause autosomal recessive spinocerebellar ataxia-27 (SCAR27) in a Chinese family

Podobne knjige/članki

• Erratum to: Reply: Novel GDAP2 pathogenic variants cause autosomal recessive spinocerebellar ataxia-27 (SCAR27) in a Chinese family
  Izdano: (2020)
• GDAP2 mutations implicate susceptibility to cellular stress in a new form of cerebellar ataxia
  od: Eidhof, Ilse, et al.
  Izdano: (2018)
• Confirming TDP2 mutation in spinocerebellar ataxia autosomal recessive 23 (SCAR23)
  od: Zagnoli-Vieira, Guido, et al.
  Izdano: (2018)
• Confirming TDP2 mutation in spinocerebellar ataxia autosomal recessive 23 (SCAR23)
  Izdano: (2018)
• Autosomal recessive spinocerebellar ataxia SCAR8/ARCA1: first families detected in Spain
  od: M. Arias, et al.
  Izdano: (2022-05-01)